hereditary oculoleptomeningeal amyloid angiopathy

Preferred Label : hereditary oculoleptomeningeal amyloid angiopathy;

Origin ID

D6-94620;

UMLS CUI

C0342609;

Automatic exact mappings (from CISMeF team)
- amyloidosis, familial visceral [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Hereditary oculoleptomeningeal amyloid angiopathy (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Non-neuropathic heredofamilial amyloidosis [ICD-10 Sub-category (who)]
Metaterm(s)
- internal medicine [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
- neurology [CISMeF Metaterm]
SNOMED CT concept
- Hereditary oculoleptomeningeal amyloid angiopathy (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary oculoleptomeningeal amyloid angiopathy (disorder) [SNOMED CT concept]